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A novel and efficient amidation of 2-aminothiazole

Authors
Choi, MinhoWon, Sun-WooJo, HyejuViji, MayavanSeo, Seung-YongLee, Yeon-JuLee, Hyi-SeungLee, HeesoonHong, Jin TaeKwak, Young-ShinJung, Jae-Kyung
Issue Date
26-Nov-2014
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Amide; 2-Aminothiazole; Carboxamide; Transamidation; t-Butylmagnesium chloride
Citation
TETRAHEDRON LETTERS, v.55, no.48, pp.6582 - 6584
Journal Title
TETRAHEDRON LETTERS
Volume
55
Number
48
Start Page
6582
End Page
6584
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12102
DOI
10.1016/j.tetlet.2014.10.031
ISSN
0040-4039
Abstract
A facile and efficient method has been developed for the synthesis of novel thiazolyl carboxamide derivatives by direct reaction of the corresponding esters and 2-aminothiazole. Treatment of 2-aminothiozole with various carboxylic esters in the presence of t-butylmagnesium chloride provides the biologically significant thiazolyl carboxamide derivatives in good to excellent yields. (C) 2014 Elsevier Ltd. All rights reserved.
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